Package 82804-129-90

Brand: nalfon

Generic: fenoprofen calcium
NDC Package

Package Facts

Identity

Package NDC 82804-129-90
Digits Only 8280412990
Product NDC 82804-129
Product ID 82804-129_01f6c461-8144-4de1-88e1-bc56defd08f3
Description

90 TABLET, FILM COATED in 1 BOTTLE (82804-129-90)

Marketing

Marketing Status
Marketed Since 2024-07-23
Brand nalfon
Generic fenoprofen calcium
Sample Package No

Linked Drug Pages (1)

NALFON ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "01f6c461-8144-4de1-88e1-bc56defd08f3", "openfda": {"upc": ["0382804129904"], "unii": ["0X2CW1QABJ"], "rxcui": ["310291", "351398"], "spl_set_id": ["01f6c461-8144-4de1-88e1-bc56defd08f3"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (82804-129-90)", "package_ndc": "82804-129-90", "marketing_start_date": "20240723"}], "brand_name": "NALFON", "product_id": "82804-129_01f6c461-8144-4de1-88e1-bc56defd08f3", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "82804-129", "generic_name": "Fenoprofen Calcium", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "NALFON", "active_ingredients": [{"name": "FENOPROFEN CALCIUM", "strength": "600 mg/1"}], "application_number": "ANDA072267", "marketing_category": "ANDA", "marketing_start_date": "20180924", "listing_expiration_date": "20261231"}